Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,728 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,728 in last 12 months

Showing 2222122240 of 30,686 recalls

Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: 1) VITROS¿ Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique...

The Issue: When testing was conducted using certain lots, VITROS¿ Systems generated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Arrow International Inc

Recalled Item: Catheter Recalled by Arrow International Inc Due to Notification of...

The Issue: Notification of component molding abnormality by supplier used to package...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: EZ adjust aluminum crutch under the following labels: 1) EZ Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Aluminum crutch under the following labels: 1) Aluminum crutch Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Arrow International Inc

Recalled Item: Catheter Recalled by Arrow International Inc Due to Notification of...

The Issue: Notification of component molding abnormality by supplier used to package...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal aluminum crutch Recalled by Medical Depot Inc. Due to Tip crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Arrow International Inc

Recalled Item: Catheter Recalled by Arrow International Inc Due to Notification of...

The Issue: Notification of component molding abnormality by supplier used to package...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Direct Supply aluminum crutch Recalled by Medical Depot Inc. Due to Tip...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing